Abstract
DNA binding regions I, II, and III at the origin of replication have different arrangements of A protein (T antigen) recognition pentanucleotides. The A protein also protects each region from DNase in distinctly different patterns. Footprint and fragment assays led to the following conclusions: (i) in some cases a single recognition pentanucleotide is sufficient to direct the binding and accurate alignment of A protein on DNA; (ii) the A protein binds within isolated region I or II in a sequential process leading to multiple overlapping areas of DNase protection within each region; and (iii) the 23-base pair span of recognition sequences in region II allows binding and protection of a longer length of DNA than the 23-base pair span in region I. We propose a model of protein binding that addresses the problem of variations in the arrangement of pentanucleotides in regions I and II and explains the observed DNase protection patterns. The central feature of the model requires each protomer of A protein to bind to a pentanucleotide in a unique direction. The resulting orientation of protein would protect more DNA at the 5' end of the 5'-GAGGC-3' recognition sequence than at the 3' end. The arrangement of multiple protomers at the origin of simian virus 40 replication is discussed.
MeSH Terms
Antigens, Viral/analysis
Antigens, Viral, Tumor
DNA Replication
DNA, Viral/analysis
Simian virus 40/genetics,immunology
Sulfuric Acid Esters
Virus Replication
Chemicals
Antigens, Viral
Antigens, Viral, Tumor
DNA, Viral
Sulfuric Acid Esters
dimethyl sulfate
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Tegtmeyer P
Lewton B A
DeLucia A L
Wilson V G
Ryder K
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21 references, click to expand
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